Taiwan FDA registration fede01c060a8277d3e5f056db168efb4
"Willette" Okrey front room analyzer
TW: “威萊特”歐克萊前房分析儀
Taiwan·Risk Class 2·WAVELIGHT GMBH·Registered Nov 29, 2011 – Nov 29, 2026ActiveRegistration details
- Analysis ID
- fede01c060a8277d3e5f056db168efb4
- Customs Code
- DHA00602303802
Company information
- Manufacturer
- WAVELIGHT GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1850 交流電力式細隙燈
- Import Information
- import
Dates and status
- Registration Date
- Nov 29, 2011
- Expiry Date
- Nov 29, 2026
About this record
Access comprehensive regulatory information for "Willette" Okrey front room analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fede01c060a8277d3e5f056db168efb4 and manufactured by WAVELIGHT GMBH. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).
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